| 2-Nitrobenzyl bromide Cov ntaub ntawv yooj yim |
| Khoom npe: |
2-Nitrobenzyl bromide |
| Synonyms: |
1-(Bromomethyl)-2-nitrobenzene;1-Bromomethyl-2-nitro-benzene; Benzene, 1-(bromomethyl)-2-nitro-;-Bromo -2-mitrotoluene;o-Nitrobenalbromide;2-NITROBENZYL BROMIDE;2-(BROMOMETHYL)NITROBENZENE;A-BROMO-O-NITROTOLUENE |
| CAS: |
3958-60-9 |
| MF: |
C7H6BrNO2 |
| MW: |
216.03 |
| EINECS: |
223-558-9 |
| Khoom Categories: |
Biochemistry; Nucleosides, Nucleotides & Related Reagents; Aromatic Halides (substituted); Tiv thaiv Agents rau Hydroxyl thiab Amino pawg; Tiv thaiv Agents, Phosphorylating Agents & Condensing Agents |
| Mol File: |
3958-60-9.mol |
 |
| |
| 2-Nitrobenzyl bromide Cov Khoom Siv Tshuaj |
| Melting point |
44-46 degree (lit.) |
| Boiling point |
265.51 degree (kev kwv yees kwv yees) |
| ceev |
1.6841 (zeeg) |
| Refractive Index |
1.6120 (kwv yees) |
| Fp |
>230 degree F |
| cia temp. |
Inert cua, 2-8 degree |
| solubility |
Chloroform (me ntsis), DMSO (me ntsis), Ethyl Acetate (me ntsis) |
| daim ntawv |
Crystalline hmoov los yog Crystalline hmoov |
| xim |
Yellow rau lub teeb xim av |
| Dej Solubility |
insoluble |
| BRN |
638991 |
| Kev ruaj ntseg: |
Hygroscopic |
| CAS DataBase Reference |
3958-60-9(CAS DataBase Reference) |
| NIST Chemistry Reference |
2-Nitrobenzyl bromide (3958-60-9) |
| |
| Cov ntaub ntawv kev nyab xeeb |
| Hazard Codes |
C |
| Risk Statements |
34 |
| Cov lus hais txog kev nyab xeeb |
26-36/37/39-45 |
| RIDADR |
UN 3261 8/PG 2 |
| WGK Germany |
3 |
| F |
4.8-19-21 |
| HazardClass |
8 |
| PackingGroup |
II |
| HS Code |
29049085 |
| Tus kws kho mob |
Lus |
| 2-Nitrobenzyl bromide |
Lus Askiv |
| ACROS |
Lus Askiv |
| SigmaAldrich |
Lus Askiv |
| ALFA |
Lus Askiv |
| |
| 2-Nitrobenzyl bromide Siv Thiab Synthesis |
| Chemical Properties |
dawb mus rau lub teeb daj crystal hmoov |
| Siv |
2-Nitrobenzyl bromide yog siv rau hauv kev npaj ntawm S-2-nitrobenzyl-cysteine los ntawm cov tshuaj tiv thaiv nrog L-cysteine. Nws kuj yog siv rau kev taw qhia ntawm 2-nitrobenzyl tiv thaiv pawg hauv organic synthesis. Nws plays lub luag haujlwm tseem ceeb hauv kev tsim cov tshuaj expectorant. Ntxiv mus, nws yog ua hauj lwm rau caging unprotected cysteine-muaj los yog thiophosphorylated peptides nyob rau hauv aqueous tov. Ntxiv rau qhov no, nws yog siv rau hauv kev npaj ntawm (R)- thiab (S)-3-amino-3, 4-dihydro-1H-quinolin{{12} }ib. |
| Siv |
2-Nitrobenzyl bromide tau siv rau caging uas tsis muaj kev tiv thaiv cysteine-muaj lossis thiophosphorylated peptides hauv cov kua dej. Nws tuaj yeem siv rau hauv kev sib txuas ntawm (R)- thiab (S) -3-amino-3, 4-dihydro-1H-quinolin-2-ib. |
| Biochem/physiol Actions |
2-Nitrobenzyl bromide reacts nrog L-cysteine rau daim ntawv S-2-nitrobenzyl-cysteine uas tau siv rau kev hloov kho ntawm ultra-low-gelling-temperature (ULGT) agarose. |
| |
| 2-Nitrobenzyl bromide Kev Npaj Khoom Siv Thiab Cov Khoom Raw |
| Cov khoom nyoos |
Carbon tetrachloride-->2,2'-Azobis(2-methylpropionitrile)-->2-Nitrotoluene-->1-(Methoxymethyl)-2-nitrobenzene |
| Cov khoom npaj |
2-NITRO-ALPHA-TOLUENESULFONYL CHLORIDE-->2,3,4,5-TETRAHYDRO-1H-BENZO[E][1,4]DIAZEPINE-->Phenyl carbamate-->2,2'-DINITRODIBENZYL |
Cim npe nrov: 2-nitrobenzyl bromide, Tuam Tshoj 2-nitrobenzyl bromide manufacturers, lwm tus neeg, Hoobkas
